Fully Registered. Fully Compliant. Fully Trusted
At Med Tech Direct, regulatory compliance isn’t just a requirement — it’s our foundation. We are fully registered and approved by all relevant New Zealand authorities governing the importation, distribution, and supply of medical technologies.
From sourcing to delivery, every product we handle is aligned with New Zealand’s strict safety, customs, and healthcare regulations — ensuring full peace of mind for institutions, clinicians, and government agencies.
Our Regulatory Registrations
Med Tech Direct Limited is:
Registered with the Medsafe WAND Database
We maintain an active registration with Medsafe’s Web-Assisted Notification of Devices (WAND) database, as required for all medical device suppliers in New Zealand. This ensures our devices are notified to the Ministry of Health and meet all relevant medical safety standards.

Aligned with NZ Customs and MPI (Ministry for Primary Industries
All imported medical technologies are cleared through New Zealand Customs and, where applicable, approved by MPI for biosecurity and product safety. We provide all required documentation, including:
  • Import declarations
  • Certificates of Origin
  • Declarations of Conformity
  • Manufacturer specifications and product labels

Registered Importer and Supplier
Med Tech Direct operates as a registered New Zealand business with official importer status for regulated medical products. We provide documentation that supports:
  • Institutional procurement
  • Government tenders
  • ACC-aligned device supply
  • Clinical usage across New Zealand
How We Ensure Compliance
Every product we supply is backed by a robust compliance and documentation process:
✔️ Verification of manufacturer certifications (ISO 13485, CE, FDA, where applicable)
✔️ Pre-import regulatory review
✔️ Full Medsafe WAND notification or guidance
✔️ Customs clearance with MPI support when needed
✔️ Labelling and documentation in line with NZ standards
✔️ Ongoing updates and traceability for each shipment
Committed to Transparency and Safety

Whether we supply a pain relief device to an ACC patient or diagnostic equipment to a hospital, we provide full visibility at every supply chain step. Our clients receive:

  • Technical documentation
  • Regulatory approval status
  • Tracking and compliance reports
  • Support for procurement applications
We work closely with customs agents, regulators, and manufacturers to ensure that every product is safe and legally compliant before it reaches our clients.
Need Documentation for a Tender?
If you're applying for a government contract or require regulatory paperwork for your organisation, we can provide:

  • Medsafe WAND registration confirmations
  • Import documentation
  • Product compliance certifications
  • Manufacturer audit histories
We’re here to support your due diligence process.
Ready to Work With a Registered Medical Importer?
Let’s discuss how we can help your team stay compliant while accessing world-class technology.

info@medtechdirect.co.nz

022 303 5496